Clinical Trials Directory

Trials / Unknown

UnknownNCT03609736

PSMA-based 18F-DCFPyL PET/CT: Evaluating Its Application in Real Life

Status
Unknown
Phase
Study type
Observational
Enrollment
12 (estimated)
Sponsor
Grand River Hospital · Academic / Other
Sex
Male
Age
18 Years
Healthy volunteers
Not accepted

Summary

The purpose of the study is to provide pilot data on the clinical situations in which ordering a 18F-DCFPyL positron emission tomography/computed tomography (PET/CT) was thought to be clinically useful, and to document how the results of the 18F-DCFPyL PET/CT affected patient management. The results of this study could then serve as a guide to help OHIP to consider these scenarios when deciding the precise indications for funded 18F-DCFPyL PET/CT scans in the future. In this study the investigators will image subjects with prostate cancer using 18F-DCFPyL PET/CT and record how the result of the study affected patient management.

Conditions

Interventions

TypeNameDescription
DIAGNOSTIC_TEST18F-DCFPyL PET/CT* A bolus of less than or equal to 9 mCi (333 MBq) of 18F-DCFPyL will be injected IV by slow IV push. * After administration of the 18F-DCFPyL the line will be flushed with saline (0.9% w/v). * Subjects should be encouraged to drink up to 500 mL of water shortly after the administration of 18F-DCFPyL. * At 60-minutes (± 10 minutes) after administration of 18F-DCFPyL, the PET/CT scan will be acquired with the subject in the supine position and the FOV including the mid-thighs to skull base.

Timeline

Start date
2018-08-10
Primary completion
2019-08-01
Completion
2019-12-01
First posted
2018-08-01
Last updated
2019-02-15

Locations

1 site across 1 country: Canada

Source: ClinicalTrials.gov record NCT03609736. Inclusion in this directory is not an endorsement.